Hydrochloric Acid → HCID 21710706, compound
Reaction equation
[ClH:1].C(OC(=O)[NH:8][CH:9]([CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[F:24])[C:10](=[O:16])[N:11]1[CH2:15][CH2:14][S:13][CH2:12]1)(C)(C)C>C(OCC)(=O)C>[ClH:1].[NH2:8][CH:9]([CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[F:24])[C:10]([N:11]1[CH2:15][CH2:14][S:13][CH2:12]1)=[O:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
HCl was bubbled into a solution of [1-(2-fluoro-benzyl)-2-oxo-2-thiazolidin-3-yl-ethyl]-carbamic acid tert-butyl ester (0.39 g, 1.1 mmol) in ethyl acetate (15 mL). The solution was concentrated, the residue was triturated in ether, the solid was filtered and dried (0.27 g, 84%, mp 217-218° C.).
Workup
- concentrationThe solution was concentrated
- customthe residue was triturated in ether
- filtrationthe solid was filtered
- customdried (0.27 g, 84%, mp 217-218° C.)
Sources & evidence
- ORD record
- ord-d239e660e380473f86cef90af7cc000f
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06107329
Reaction notes
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